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Hyperpolarized Imaging for New Treatments

Study acronym: HyPOINT
StatusCompleted
PhasePhase 4
Started
View on ClinicalTrials.gov ↗

Record History

  1. Notable Lead sponsor: Children's Hospital Medical Center, Cincinnati to Children's Hospital Medical Center, Cincinnati Trial completed · Final enrollment: 47 participants (planned 64) · Primary completion date changed from estimate of Sep 10, 2026 to May 1, 2026 · 4 more Show 7 more changesShow less
    • Trial completed
    • Final enrollment: 47 participants (planned 64)
    • Primary completion date changed from estimate of Sep 10, 2026 to May 1, 2026
    • Eligibility criteria expanded, about 16 words
    • Secondary endpoints: details revised at 2 of 3 entries
    • Site details revised at 1 of 4 sites
    • Publications: details revised at 1 of 1 entry
  2. Minor Primary completion pushed from May 1, 2026 to Sep 10, 2026 Completion pushed from Dec 31, 2026 to May 1, 2027v10 Show 1 more changeShow less
    • Completion pushed from Dec 31, 2026 to May 1, 2027
  3. Minor Primary completion date: Dec 31, 2025 to May 1, 2026 Completion date: Dec 31, 2025 to Dec 31, 2026v9 Show 1 more changeShow less
    • Completion date: Dec 31, 2025 to Dec 31, 2026
  4. Minor Re-verified, no change to tracked fieldsv8
  5. Minor Primary and study completion dates: Dec 2025 to Dec 31, 2025v7
Show 5 earlier versionsHide 5 earlier versions
  1. Minor Trial status: Recruiting to Active, Not Recruiting Site details revised at 4 of 4 sitesv6 Show 1 more changeShow less
    • Site details revised at 4 of 4 sites
  2. Minor Re-verified, no change to tracked fieldsv5
  3. Minor Eligibility criteria expanded, about 3 wordsv4 See this version in full on ClinicalTrials.gov ↗
  4. Notable Enrollment target: 40 to 64v3
  5. Minor Study sites: 1 to 4v2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The introduction of triple combination CFTR modulator therapy for patients with Cystic Fibrosis (CF) with at least one copy of the deltaF508 mutation is expected to provide major health benefits, but will also require novel outcome measures that can detect CF lung disease at an early stage, capture the efficacy of new therapies when disease manifestations are limited, as well as determine whether stopping existing chronic maintenance therapies does not have negative effects. In the past decade, research has focused on the multiple breath washout (MBW) test, as a sensitive outcome measure, especially if highly-effective modulator therapies are initiated in early childhood. Even LCI, however, may not adequately capture early lung function changes, thus warranting investigation of even more sensitive outcome measures. Magnetic resonance imaging (MRI) has the advantage of being a radiation-free modality, making it more suitable for assessing response to therapy in a shorter time frame with repeated imaging. Inhalation of a hyperpolarized gas enables the visualization and quantification of regional ventilation in the lung and can be combined with structural MRI to assess both structure and function in parallel. The main Investigator and others have recently formed an international consortium (the 129Xe MRI Clinical Trial Consortium), comprised of both imaging experts and pulmonary clinicians to standardize imaging procedures, thus facilitating multi-site implementations. Data from this proposed study (HyPOINT; Hyperpolarized Imaging for New Treatments) will inform the future utility of MRI for both longitudinal studies to track disease progression over time as well as for future interventional trials. Further, the current study could inform the design of future trials of interventions of patients for whom currently no effective CFTR modulator therapy is available and for patients with rare genotypes thus laying the groundwork for a more personalized medicine approach in the near-term future.
Trial Details
NCT Number NCT04259970
Lead Sponsor Children's Hospital Medical Center, Cincinnati
Collaborators: University of Virginia, University of Wisconsin, Madison, The Hospital for Sick Children
Conditions Cystic Fibrosis
Enrollment 47 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov